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HRID 509136作成日:2026年10月24日

1-Methylimidazole → (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide

https://huagongshe.com/ja/reaction/509136

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylimidazoleHCID 1390—
反応物Thionyl ChlorideHCID 24386—
反応物3-Benzoylpropionic acidHCID 72871—
反応物(S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamineHCID 57943187—
溶媒DichloromethaneHCID 6344—
生成物(S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamideHCID 59464671—

反応手順

3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of thionyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096555B2
出典データセットuspto-grants-2015_08
ORD IDord-ff49d2f1be53475c8f3970b1bcfafb0e
出典メモuspto-grants-2015_08